If you need hernia mesh claim advice having suffered from complications, you can contact our specialist team for help.
We’re already involved in legal action for victims claiming damages for vaginal mesh implant problems. We can now also take cases forward for hernia mesh complications as well.
The Group Action Lawyers are fighting in over 30 different group legal actions. Millions of pounds have been recovered for victims across a broad range of cases, with £1.3m recovered so far alone in the PIP breast Implant scandal.
If you need to make a hernia mesh claim, our lawyers can help you now.
A large number of vaginal mesh lawsuits are already being pursued, and if you need advice for starting yours, you can contact the team for advice today.
Thousands of women have reported suffering from mesh implant complications, and the UK has been slow to take real action to safeguard women and ensure compensation is awarded for victims who are now suffering.
Some of the problems people can suffer from can be irreversible, so it’s important for anyone suffering with complications to start their vaginal mesh lawsuit as soon as they can; especially given that time limitations for new cases can be tricky.
A Latanoprost Timolol eye drops recall has been announced by the Medicines and Healthcare Regulatory Authority (MHRA).
The company behind the eye drops, FDC Pharma, are recalling a batch due to what has been classed as an ‘out of specification result for an unknown impurity’ that was identified during testing. Medical professionals are to stop providing the eye drops to patients, and suppliers and distributors are to cease moving the eye drops as well.
The NHS has been pushing the news throughout the Service to ensure batches affected by the Latanoprost Timolol eye drops recall are not used.
One of the latest talcum powder asbestos trial cases is underway as a 94-year-old lady is claiming that her fatal mesothelioma was caused by talc.
This is one of the many cases being pursued in an action where millions of pounds have been awarded to victims who have successfully claimed that their deadly asbestos-related illnesses have been caused by talcum powder containing the deadly substance.
The talcum powder asbestos action is one of the biggest medical product issues of our time, and it could be set to go on for a number of years.
Pelvic mesh suits are to continue against pharmaceutical giant Boston Scientific after a Judge denied an attempt to dismiss some 800 claims.
The major pharmaceutical companies like Boston Scientific and Johnson and Johnson seem to be trying their hardest to dismiss the thousands of claims that are currently being made against them in them around the world. The UK is somewhat behind in terms of taking full legal action for victims pursuing pelvic mesh suits, and it’s a legal action we’re involved in.
This latest failed effort to dismiss claims is another small victory in what continues to be a long, hard fight for justice.
The increasing number of pelvic mesh implant complications has finally forced the NHS to put a widespread halt on the use of the procedure as more and more women come forward with problems over the use of transvaginal mesh and transvaginal tape.
We’ve been advising women suffering mesh implant complications since the start of 2013, and our Group Action Lawyers are involved in legal action over the use of the devices. We wholeheartedly welcome the NHS pause on the use of the implants that’s arisen from a review chaired by Baroness Julia Cumberlege.
This may prove to be another crucial step forward toward justice for the many women who have suffered catastrophic and lifelong injuries caused by mesh implant complications.
There has been an immediate discontinuation of unlicensed medicine Phenytoin 90mg/5ml Oral Suspension and a recall of the product.
The medication, manufactured by Rosemont Pharmaceuticals Limited, is now no longer on the shelves having been recalled and discontinued with immediate affect as a result of worrying data that suggested that the medication becomes difficult to resuspend over shelf-life.
Patients who use the Phenytoin 90mg/5ml Oral Suspension are being told to contact their doctors for more information and advice about the issues that have been identified.
Roche Diabetes Care test strip errors has led to a recall of a number of home-use and point-of-care glucose monitoring systems.
The Roche Diabetes Care test strip errors are for the following systems: Accu-Chek Aviva; Accu-Chek Performa; and Accu-Chek Inform II.
There is a risk of a strip error message that may lead to either falsely high or falsely low blood glucose results reported.
A troubling testimony in the Gosport War Memorial Hospital deaths has been recounted in the recent independent inquiry that deemed some 450 deaths at the hospital were linked to an unsafe opioid-use policy.
Families who have been fighting for an inquiry for years have finally received the news that they say they knew all along: that their loved-ones died in the hospital prematurely.
At the centre of the Gosport War Memorial Hospital deaths scandal is Dr Jane Barton; the GP stationed there who claims that she was only ever doing the best for her patients. One particularly troubling testimony from 2001 that was recounted in the independent report paints a different story entirely.
According to an independent report, 450 Gosport hospital deaths could have been avoided after life-shortening opioids were reportedly given to elderly patients who did not need them.
The damning report found that a GP working at the hospital, Dr Jane Barton, routinely overprescribed drugs to patients in the 1990s, and consultants who were aware of her actions did not intervene. Further, nurses and pharmacists would have known that the high levels of opioids administered would not always have been appropriate, and they too failed to stop the deaths.
After years of the families campaigning and suffering over the Gosport hospital deaths, the report has finally confirmed what they already knew.
News of a diabetes testing kit recall is said to be “urgent” amid fears of lives at risk over false readings.
The Accu-Chek Aviva and the Accu-Chek Performa are the diabetes testing kits being recalled that could lead to an overdose or an under-dose of insulin that can lead to serious health complications for users.
Advice to patients is to stop using the affected devices and return them to a pharmacy for a replacement.
A J & J subsidiary companied is reportedly being sued for breast implants causing cancer. According to the legal case, a Johnson & Johnson subsidiary company who has manufactured breast implants for some 5 million women has left at least one woman with breast cancer.
It’s alleged that the Claimant developed breast implant-associated anaplastic large-cell lymphoma, which is a rare form of T-cell lymphoma. She alleges that the cause of her cancer stems from being fitted with MemoryGel Siltex breast implants that are manufactured by Mentor Worldwide LLC; a subsidiary company of J & J.